drugset / Trial / NCT03343639
Study of the Efficacy, Safety and Tolerability of Serlopitant for the Treatment of Pruritus (Itch) With Plaque Psoriasis
RandomizedParallel-groupQuadruple-blindTreatment
Summary
Study of the efficacy, safety, and tolerability of serlopitant for the treatment of pruritus in adults with plaque psoriasis
Timeline
- Start
- 2017-11-01
- Primary completion
- 2018-10-23
- Completion
- 2018-11-12
Outcome
Met primary endpoint
paper The WI-NRS 4-point response rate at 8 weeks (primary end point) was 33.3% for serlopitant vs 21.1% for placebo (P = .028); PMID 32007513 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Serlopitant | Small molecule | 5 mg | Oral |